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Prophylactic and long-lasting efficacy of senolytic CAR T cells against age-related metabolic dysfunction

  • Corina Amor,
  • Inés Fernández-Maestre,
  • Saria Chowdhury,
  • Yu-Jui Ho,
  • Sandeep Nadella,
  • Courtenay Graham,
  • Sebastian E. Carrasco,
  • Emmanuella Nnuji-John,
  • Judith Feucht,
  • Clemens Hinterleitner,
  • Valentin J. A. Barthet,
  • Jacob A. Boyer,
  • Riccardo Mezzadra,
  • Matthew G. Wereski,
  • David A. Tuveson,
  • Ross L. Levine,
  • Lee W. Jones,
  • Michel Sadelain,
  • Scott W. Lowe

摘要

Senescent cells, which accumulate in organisms over time, contribute to age-related tissue decline. Genetic ablation of senescent cells can ameliorate various age-related pathologies, including metabolic dysfunction and decreased physical fitness. While small-molecule drugs that eliminate senescent cells (‘senolytics’) partially replicate these phenotypes, they require continuous administration. We have developed a senolytic therapy based on chimeric antigen receptor (CAR) T cells targeting the senescence-associated protein urokinase plasminogen activator receptor (uPAR), and we previously showed these can safely eliminate senescent cells in young animals. We now show that uPAR-positive senescent cells accumulate during aging and that they can be safely targeted with senolytic CAR T cells. Treatment with anti-uPAR CAR T cells improves exercise capacity in physiological aging, and it ameliorates metabolic dysfunction (for example, improving glucose tolerance) in aged mice and in mice on a high-fat diet. Importantly, a single administration of these senolytic CAR T cells is sufficient to achieve long-term therapeutic and preventive effects.